Canonical Allele Identifier: CA2677794920

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29944598-TGGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944605_29944607del , CM000668.2:g.29944605_29944607del	GRCh38
NC_000006.11:g.29912382_29912384del , CM000668.1:g.29912382_29912384del	GRCh37
NC_000006.10:g.30020361_30020363del	NCBI36
NG_029217.2:g.7141_7143del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.895+208_895+210del	ENSP00000492789.2:n.895+208_895+210del
ENST00000706892.1:n.1957_1959del
ENST00000706893.1:c.1035_1037del	ENSP00000516609.1:p.Glu346del
ENST00000706894.1:c.1001_1003del	ENSP00000516610.1:p.Arg334del
ENST00000706895.1:n.1379_1381del
ENST00000706896.1:n.1855_1857del
ENST00000706897.1:n.1277_1279del
ENST00000706898.1:c.1001_1003del	ENSP00000516611.1:p.Arg334del
ENST00000706899.1:n.1855_1857del
ENST00000706900.1:c.917_919del	ENSP00000516617.1:p.Arg306del
ENST00000706901.1:c.1001_1003del	ENSP00000516612.1:p.Arg334del
ENST00000706902.1:c.1001_1003del	ENSP00000516613.1:p.Arg334del
ENST00000706903.1:c.1001_1003del	ENSP00000516614.1:p.Arg334del
ENST00000706904.1:c.1001_1003del	ENSP00000516615.1:p.Arg334del
ENST00000706905.1:c.1001_1003del	ENSP00000516616.1:p.Arg334del
ENST00000376809.10:c.1001_1003del MANE Select	ENSP00000366005.5:p.Arg334del
ENST00000638375.1:c.895+208_895+210del	ENSP00000492789.1:n.895+208_895+210del
ENST00000376802.2:c.895+208_895+210del	ENSP00000365998.2:n.895+208_895+210del
ENST00000376806.9:c.1001_1003del	ENSP00000366002.5:p.Arg334del
ENST00000376809.9:c.1001_1003del	ENSP00000366005.5:p.Arg334del
ENST00000396634.5:c.1001_1003del	ENSP00000379873.1:p.Arg334del
ENST00000461903.1:n.1242_1244del
ENST00000479320.5:n.1242_1244del
ENST00000495183.5:n.1244_1246del
ENST00000496081.5:n.818_820del
NM_002116.7:c.1001_1003del	NP_002107.3:p.Arg334del
NM_002116.8:c.1001_1003del MANE Select	NP_002107.3:p.Arg334del